The inherited bone marrow failure syndromes - Test2 - elhamkhani - TriplyDB

The inherited bone marrow failure syndromes

The inherited bone marrow failure syndromes

http://www.wikidata.org/entity/Q26999046

about

The role of human cervical cancer oncogene in cancer progression A Comprehensive Review of Pediatric Tumors and Associated Cancer Predisposition Syndromes.Thrombocytopenia absent radius syndrome with Tetralogy of Fallot: a rare association.Global transcriptome analyses of human and murine terminal erythroid differentiation.FANCD2 functions as a critical factor downstream of MiTF to maintain the proliferation and survival of melanoma cells Bypass of the pre-60S ribosomal quality control as a pathway to oncogenesis.Stress and DNA repair biology of the Fanconi anemia pathway Case 1: A newborn with pancytopenia.Diagnosis and management of congenital dyserythropoietic anemias.The Contributions of the Ribosome Biogenesis Protein Utp5/WDR43 to Craniofacial Development

P2860

Q26796977-E4A6F967-D20B-432B-9F4E-453CE79CA358 Q30252766-4749C11F-49EC-47FF-8C4E-E63A93C29995 Q33422293-8B0DB685-C176-42FD-881C-11F7C3FB3484 Q33697238-8D0782E6-E512-4341-AAD5-8A65494622C3 Q37402621-ECB7B844-CB50-4D52-9C77-C15346E4360D Q37711977-A165223B-C19D-4295-9A9E-4F1781D29544 Q38252562-9CE1CB21-5D7D-4F89-9B29-5C77DE6E8C60 Q38544673-A04A9D08-4613-4F9F-A209-127466DEC9FC Q38664955-FA8919BC-FB03-4ACE-A7DB-F25797DBB0C4 Q38843526-7F8FCA75-3132-4306-8813-D280F8B38B2B

P2860

The inherited bone marrow failure syndromes

http://www.wikidata.org/entity/Q26999046

description

2013 nî lūn-bûn

@nan

2013 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2013年の論文

@ja

2013年論文

@yue

2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

name

The inherited bone marrow failure syndromes

@ast

The inherited bone marrow failure syndromes

@en

The inherited bone marrow failure syndromes

@nl

type

label

The inherited bone marrow failure syndromes

@ast

The inherited bone marrow failure syndromes

@en

The inherited bone marrow failure syndromes

@nl

prefLabel

The inherited bone marrow failure syndromes

@ast

The inherited bone marrow failure syndromes

@en

The inherited bone marrow failure syndromes

@nl

P1433

Q26999046-D914A0B5-64A0-45FD-9282-3056AC6B8DF1

P1476

Q26999046-19C5B0DA-824E-4BE6-939D-289B456B5958

P2093

Q26999046-79D7B339-CB63-4CF2-8E03-4A9B4DC12F2E

Q26999046-7B73792C-EE89-497D-9240-E78917E8F8FF

P2860

Q26999046-03AECC26-7371-4979-BA9D-2AC607AF8B8B

Q26999046-048590AB-8BE7-452C-BFF2-E06D774BC06E

Q26999046-0841A9DB-54CB-4282-BEA9-4E3B96AECC6E

Q26999046-08A2EF26-92C5-408F-AA3F-3679DC611F66

Q26999046-08F96CFE-455D-4950-8759-D87D92688B98

Q26999046-095ED04B-83A9-41A7-8C01-930D7C4ECEAE

Q26999046-0C6B82D9-47AF-4FB2-BD32-DDE87C104EED

Q26999046-0E8EABB9-518B-4C2F-8A0F-53F05CBFCB56

Q26999046-0F496FDE-7BB1-41C5-BBD3-1757C6B3FFAE

Q26999046-1006466D-428A-4787-B46E-3E5315489ED1

P304

Q26999046-4B8BAD2B-563F-426C-90B7-3A720C0403F4

P31

Q26999046-BB068CCD-BAC5-4A44-B2B8-0B89BFAFA600

P3181

Q26999046-A33160F4-4B9D-4CA9-A76D-F7C0842DCA70

P356

Q26999046-003EAB30-C922-4D9E-ACF5-CF18091DB39F

P407

Q26999046-B8F04C2D-AF18-4D48-B249-5EC149971FEC

P433

Q26999046-C741755D-7773-4ECE-97B9-B1B6EB69F7CD

P478

Q26999046-E89985F1-009D-4DB4-9CD9-CA7A0EEE93F6

P577

Q26999046-2D0378A1-7E9D-4115-A875-344D529399BF

P698

Q26999046-1A736BB2-A05F-4D5D-97ED-C83B9D35C312

P921

Q26999046-87C2A9F5-4BE8-46A6-BE69-4443804DA889

P932

Q26999046-77C9ECE2-597A-458D-8E7F-583B6FA6F0B5

P3181

P356

J.PCL.2013.09.007

P1433

Pediatric Clinics of North America

P1476

The inherited bone marrow failure syndromes

@en

P2093

Gary M. Kupfer

http://www.w3.org/2001/XMLSchema#string

S. Deborah Chirnomas

http://www.w3.org/2001/XMLSchema#string

P2860

Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1{alpha} localization in erythroblasts

A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia

An RNA-dependent RNA polymerase formed by TERT and the RMRP RNA

The genetics of dyskeratosis congenita

Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1

Molecular pathogenesis and clinical management of Fanconi anemia

Squamous cell carcinomas of the head and neck in Fanconi anemia: risk, prevention, therapy, and the need for guidelines

Mutations in ribosomal protein S19 gene and diamond blackfan anemia: wide variations in phenotypic expression

Mutations in the RNA component of RNase MRP cause a pleiotropic human disease, cartilage-hair hypoplasia

Fanconi anemia group C protein prevents apoptosis in hematopoietic cells through redox regulation of GSTP1

P304

1291-310

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P3181

2618503

http://www.w3.org/2001/XMLSchema#string

P356

10.1016/J.PCL.2013.09.007

http://www.w3.org/2001/XMLSchema#string

P407

P433

6

http://www.w3.org/2001/XMLSchema#string

P478

60

http://www.w3.org/2001/XMLSchema#string

P577

2013-12-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

24237972

http://www.w3.org/2001/XMLSchema#string

P921

P932

3875142

http://www.w3.org/2001/XMLSchema#string